EP0155140A2

EP0155140A2 - Compositions based on 1,1,2-Trichlorotrifluoroethane for industrial washing

Info

Publication number: EP0155140A2
Application number: EP85301526A
Authority: EP
Inventors: Gianangelo Bargigia; Mauro Scapin
Original assignee: Montefluos SpA; Ausimont SpA
Current assignee: Solvay Specialty Polymers Italy SpA
Priority date: 1984-03-07
Filing date: 1985-03-06
Publication date: 1985-09-18
Anticipated expiration: 2005-03-06
Also published as: ES540980A0; EP0155140B1; US4620946A; ATE57397T1; CA1235353A; JPS60217300A; ES8706198A1; IT8419925A0; IT1175805B; EP0155140A3; DE3580053D1

Abstract

Compositions suitable to be used for washing industrial materials, comprising, by weight:63 - 98.9% of 1,1,2-trichlorotrifluoroethane;0.5 - 25% of water;0.6-12% of a mixture of 80-97% by weight of a compound of formula (I) and of 20-3% by weight of a compound of formula (II); wherewherein: R = a C9 - C15 alkyl groupA = a C2-C8 aliphatic or cyclic amine, a diamine, or a polyamine; and(II) is X-(CO)n-OH wherein: n = 0 or 1X = a C6-C25 alkyl or an alkylene group.

Description

The present invention relates to compositions based on 1,1,2-trichlorotrifluoroethane (R113, according to the international nomenclature of refrigerants) suitable to be used as means for industrial washing.
The properties of the chlorofluorinated solvents, in particular those of 1,1,2-trichlorotrifluoroethane, for removing oily and fatty substances from the surfaces of metal and/or plastic objects, coming from intermediate stages of processing, are known, as is the sensitivity of such solvents towards construction materials.
For these reasons the use of such solvents has increased considerably and has become an important part of the processing of various objects, such as the fields of electronics, fine mechanics, optics, jewellery, and galvanics. For particular cases, special mixtures were formulated wherein, to the main chlorofluorocarbon component, other solvents were added, capable of imparting particular properties without however changing the essential characteristics of the main component. For instance, azeotropic mixtures of 1,1,2-trichlorotrifluoroethane-methanol; 1,1,2-trichlorotrifluoroethane-ethanol; 1,1,2-trichlorotrifluoroethane-isopropanol; and 1,1,2-trichlorotrifluoroethane-methylene chloride have been described.
In the particular case of 1,1,2-trichlorotrifluoroethane, a mixture thereof with water was also suggested. so that, in washing operations, it was possible to remove by means of a single operation, in addition to dirt of a fatty nature, dirt of a salty nature as well.
Since, however, a simple physical mixture was not suited to the purpose, there were added particular surfactants which, by promoting the formation of stable emulsions of the water in oil type, gave rise to efficacious limpid mixtures.
In this connection the use was described, as surfactants, of isopropylammonium dodecylbenzenesulfonate (British Patent No. 1,019.859), of aminic salts of undecyl - or tridecylbenzenesulfonic acids (British Patent No. 1,258,757), of mixtures of salts of alkyl and dialkyl phosphoric acids and amines (British Patent No. 1.499.271) and lastly of sodium, ammonium or alkylammonium salts of mono-sulfonic acid obtained from the diester of a succinic acid (British Patent No. 1,157,190).
The hitherto used surfactants, however, have the drawback of not fulfilling completely the requirements of biodegradability, or are obtainable only with difficulty, or are expensive as far as their preparation is concerned.
One aim of the present invention is to provide a composition for industrial washing the elimination of which does not cause environmental or pollution problems.
Another aim of the present invention is to provide a composition for industrial washing which utilizes a lower amount of a same surfactant while giving an equally effective performance.
The present invention provides a washing composition comprising 1.1,2-trichlorotrifluoroethane and water, together with an additive comprising a mixture of (i) an alkylammonium benzenesulfonate of general formula:
wherein: R is a linear or branched alkyl group having from 9 to 15, but preferably from 11 to 13, carbon atoms; and A may be:

(a) a primary, secondary, or tertiary, linear or branched, aliphatic or cyclic amine, having from 2 to 8 carbon atoms, preferably a branched primary aliphatic amine containing 3 or 4 carbon atoms, or a primary cyclic amine; or
(b) a diamine of general formula
wherein: B is an alkylene group containing from 3 to 12 carbon atoms, or
(c) a polyamine of general formula:
wherein:
- m is an integer from 1 and 4,
- with (ii) at least one compound (defined as coadjuvant agent) of general formula (II) X-(CO)_n -OH
- wherein n is 1 or zero and wherein X is a linear, branched or cyclic alkyl or alkylene group having from 6 to 25 carbon atoms, preferably from 8 to 20 carbon atoms.

In particular, such a mixture, that forms the additive, comprises from 80% to 97%, preferably from 88% to 94%, by weight of at least one compound of formula (I) and from 20% to 3%, preferably from 12 to 6%, by weight of at least one compound of general formula (II).
Therefore, the washing compositions, of the present invention, comprise:

(a) from 63% to 98.9% preferably from 79% to 97.5%, by weight of 1,1,2-trichlorotrifluoroethane;
(b) from 0.5% to 25%, preferably from 1.5 to 15%. by weight of water;
(c) from 0.6% to 12%, preferably from 1% to 6%, by weight of a mixture of 80%-97% by weight of at least one compound of formula (I) and of 20%-3% by weight of at least one compound of formula (II).

Preferably, in general formula (I), R is an undecyl, dodecyl. or tridecyl radical, linear or branched, and A is isopropylamine or t. butylamine.
The compounds of formula (II) include the saturated or unsaturated, linear, branched or cyclic, carboxylic acids, among which the saturated or unsaturated, linear or branched fatty acids having from 12 to 18 carbon atoms are particularly preferred.
The linear or branched aliphatic or cycloaliphatic alcohols are included in said formula (II) as well. Among them, alcohols containing from 8 to 16 carbon atoms are particularly preferred.
Typical examples of compounds of general formula (II) are: 5-decanol, 1-dodecanol, 1-octadecanol, 1-tetradecanol, cyclohexanol, methylcyclohexanol, 5-nonanol, 2-octanol, myristic acid, oleic acid, and cyclohexanecarboxylic acid, and preferably: 1-octanol, 1-hexadecanol, 1-nonanol, stearic acid, lauric acid, 9-octadecene-l-ol, and 1-decanol.
The compositions according to the invention retain water in the form of an emulsion, stable in time and they do not undergo any adverse alteration due to the addition of optional substances, such as nitromethane, introduced as stabilizing agents, if required by the materials to be washed.
The manners of employing the compositions according to the present invention are analogous to those already known for products which are presently commercially available. The same considerations also apply as far as the nature of the objects to be washed is concerned.
The invention will be further described with reference to the following illustrative Examples. The tests are carried out at room temperature, unless otherwise specified.

EXAMPLE 1

Isopropylammonium dodecylbenzenesulfonate was prepared by employing isopropylamine and a dodecylbenzenesulfonic acid produced by the Marchon Company, characterized (through ¹HNMR test) by having a ratio: H atoms on CH₃/total a liphatic H atoms = 0.24 and moreover by having a biodegrad ability of 99.0% (according to the rules of minsterial dec ree of July 19, 1974.).
This preparation was carried out by mixing equimolecular amounts of the reactants, both of them dissolved at 20% in trichlorotrifluoroethane, and by evaporating the solvent.
Weighed amounts of the dodecylbenzenesulfonate prepared as described hereinbefore and 1-decanol, the latter in an amount by weight equal to 10/90 of the dodecylbenzenesulfonate, were introduced into a 100 ml flask. Then sufficient 1,1,2-trichlorotrifluoroethane was added to achieve a weight of 100g and the whole was stirred until dissolution occurred.
Keeping the solution under stirring, by means of a graduated burette, deionized water was added slowly until it was dissolved, the addition of water being stopped when a stable opalescence appeared.
By proceeding exactly as described hereinbefore, the test was repeated without addition of 1-decanol.
The results of the tests carried out are given in Tables I and II below:

EXAMPLE 2

Solutions in 1,1,2-trichlorotrifluoroethane of the same isopropylammonium dodecylbenzenesulfonate and of the same 1-decanol were prepared as described in example 1. In each test the solutions contained 1% by weight of an additive consisting of mixtures of dodecylbenzenesulfonate and 1-decanol, respectively in ratios by weight of 100/0; 99/1; 95/5; 90/10.
The amount of water emulsifiable by each solution is given in the Table III below.

EXAMPLE 3

Additives were prepared consisting of 90 parts by weight of the same sulfonic surfactant as used in example 1 and 10 parts by weight of various coadjuvant agents.
Into a 100ml flask, containing 98g of 1,1,2-trichlorotrifluoroethane and 2g of additive, kept under stirring, water was added until saturation.
The obtained results are given in Table IV below.

EXAMPLE 4

From the same dodecylbenzenesulfonic acid as used in example 1 and terbutylamine, the respective dodecylbenzenesulfonate was prepared.
Following the conditions of example 3, a solution was prepared, in 1,1,2-trichlorotrifluoroethane, of the additive consisting of terbutylammonium dodecylbenzenesulfonate and 1-decanol and the amount of emulsifiable water was measured.
The same test was repeated without using 1-decanol.
The obtained results are given in Table V below.

EXAMPLE 5

There was followed the procedure as described in example 1 with the difference that use was made of a dodecylbenzenesulfonic acid characterized by having a ratio: H atoms on CH₃/total aliphatic H atoms = 0.41, as determined through ¹H NMR, and characterized by having a biodegradability of 80.0%.
The test results are given in Tables VI and VII below.

EXAMPLE 6

There was followed the procedure as described in example 1 with the difference that use was made of a dodecylbenzenesulfonic acid produced by the Arca Company, characterized by having a ratio: H atoms on CH₃/total aliphatic H atoms = 0.24, as determined through ¹H NMR, and characterized by having a biodegradability of 99.0%.
The test results are given in the following Tables VIII and IX below.

EXAMPLE 7

A suitable tank of an ultra-sound machine for washing objects of small size was filled with the composition described in Test 2 of example 6.
After having started the ultra-sound generator, by means of a small stainless steel object-supporting basket or by means of hooks, the following objects were introduced:

1. Metal, brass or stainless steel pieces, coming from turning operations and sprinkled during the processing with an emulsion mineral oil/network water used as a lubricating and refrigerating agent.
2. Slides for microscopes and optical lenses with signs of fingerprints; slides for microscopes dirtied purposely by immersion into concentrated salt solutions and, after drying, furthermore dirtied with mineral oil.
3. A Bremas commutator model 10A, after having been used and disassembled for overhauling.
4. An auxiliary relay with 5 commutating contacts, RIA - MTI - Italy make, after having been used and disassembled for overhauling.
5. A Siemens temperature relay, after having been used and disassembled for overhauling.
6. A one-phase asynchronous motor, Arduini make, after having been used and disassembled for overhauling.
7. A type-holder device of an Olivetti typewriter.

The time required for washing varied from one to five minutes, depending on the complexity and on the dirt degree of the piece.
After the washing operation the pieces were rinsed twice in pure 1,1.2-trichlorotrifluoroethane, kept at boiling temperature, and lastly they were kept for about one minute within the solvent vapours.
All the pieces thus treated were found to be perfectly clean. Pieces 3, 4, 5, 6 after having been reassembled in their respective electric circuits, ran regularly.

Claims

1. A composition suitable to be used for industrial washing, characterized by comprising, by weight:

a) from 63% to 98.9 % of 1,1,2-trichlorotrifluoroethane;

b) from 0.5% to 25% of water;

c) from 0.6% to 12% of a mixture of 80-97% by weight of at least one compound of formula:
(I) R-C₆H₅-SO₃H.A wherein R is a linear or branched alkyl group having from 9 to 15 carbon atoms, and A is

(i) a primary, secondary or tertiary, linear or branched, aliphatic or cyclic amine having from 2 to 8 carbon atoms; or

(ii) a diamine of general formula ^H ₂N-B-NH₂ wherein: B is an alkylene group containing from 3 to 12 carbon atoms; or

(iii) a polyamine of general formula NH₂-CH₂-CH₂-(NH-CH₂-CH₂)_m -NH₂ wherein m is an integer from 1 to 4; with 20%-3% by weight of at least one compound cf formula:
(II) X-(CO) _n-OH wherein n is 1 or zero and wherein X is a linear, branched or cyclic alkyl or alkylene group having from 6 to 25 carbon atoms.

2. A composition as claimed in claim 1, characterized in that the amount of said component (c) is from 1% to 6% by weight.

3. A composition as claimed in claim 1 or 2, characterized in that the amount of said component (a) is from 79% to 97.5% by weight.

4. A composition as claimed in any of claims 1 to 3, characterized in that the amount of said component (b) is from 1.5% to 15% by weight.

5. A composition as claimed in any of claims 1 to 4, characterized in that said component (c) comprises from 88% to 94% by weight of at least one compound of formula (I) and from 12% to 6% by weight of at least one compound of formula (II).

6. A composition as claimed in any of claims 1 to 5, characterized in that, in the compound(s) of formula (I) , R is an undecyl, dodecyl or tridecyl radical and A is isopropylamine or t.butylamine.

7. A composition as claimed in any of claims 1 to 6, characterized in that the said at least one compound of formula (II) is a linear or branched, saturated or unsaturated, fatty carboxylic acid having from 12 to 18 carbon atoms.

8. A composition as claimed in any of claims 1 to 6, characterized in that the said at least one compound of formula (II) is an aliphatic or cycloaliphatic alcohol having from 8 to 16 carbon atoms.